Linlin Wang

Guangxi Key Laboratory Of Birth Defects Research And Prevention, Guangxi Key Laboratory Of Reproductive Health And Birth Defects Prevention
Nanning, China

Last Updated: 09/26/2026

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Found 10 publications

Novel Compound Heterozygous Variants in the COG5 Gene Causing Fetal Hydrops and Skeletal Dysplasia.

Novel Compound Heterozygous Variants in the COG5 Gene Causing Fetal Hydrops and Skeletal Dysplasia.

Journal: Molecular genetics & genomic medicine
Published: November 20, 2025

The values of the cardio-biparietal ratio and cardio-femur ratio in predicting homozygous α-thalassemia-1 fetuses in early and mid-pregnancy.

The values of the cardio-biparietal ratio and cardio-femur ratio in predicting homozygous α-thalassemia-1 fetuses in early and mid-pregnancy.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
Published: November 09, 2025

16p13.11 deletion/duplication: a large cohort study on prenatal diagnosis, postnatal outcomes, and phenotypic manifestations.

16p13.11 deletion/duplication: a large cohort study on prenatal diagnosis, postnatal outcomes, and phenotypic manifestations.

Journal: BMC pregnancy and childbirth
Published: July 06, 2025

Clinical and Molecular Characterization of Five Additional Individuals With SATB2-Associated Syndrome in Guangxi.

Clinical and Molecular Characterization of Five Additional Individuals With SATB2-Associated Syndrome in Guangxi.

Journal: Biochemical genetics
Published: June 09, 2025

Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience.

Clinical and genetic profiles of postnatal patients with skeletal dysplasia in Guangxi during 8 years: a single-center experience.

Journal: Orphanet journal of rare diseases
Published: May 20, 2025

The Genetics of 241 Fetuses With Talipes Equinovarus: A 8-Year Monocentric Retrospective Study.

The Genetics of 241 Fetuses With Talipes Equinovarus: A 8-Year Monocentric Retrospective Study.

Journal: Molecular genetics & genomic medicine
Published: August 13, 2024

Identification of a novel FERMT1 variant causing kindler syndrome and a review of the clinical and molecular genetic features in Chinese patients.

Identification of a novel FERMT1 variant causing kindler syndrome and a review of the clinical and molecular genetic features in Chinese patients.

Journal: Frontiers in pediatrics
Published: April 29, 2024

Prenatal chromosomal microarray analysis and karyotyping in fetuses with isolated choroid plexus cyst: A retrospective case-control study.

Prenatal chromosomal microarray analysis and karyotyping in fetuses with isolated choroid plexus cyst: A retrospective case-control study.

Journal: European journal of obstetrics, gynecology, and reproductive biology
Published: December 21, 2023

A genetic variant in the MAST1 gene is associated with mega-corpus-callosum syndrome with hypoplastic cerebellar vermis, in a fetus.

A genetic variant in the MAST1 gene is associated with mega-corpus-callosum syndrome with hypoplastic cerebellar vermis, in a fetus.

Journal: Molecular genetics & genomic medicine
Published: June 27, 2023

Etiology and Perinatal Outcome of Nonimmune Hydrops Fetalis in Southern China.

Etiology and Perinatal Outcome of Nonimmune Hydrops Fetalis in Southern China.

Journal: AJP reports
Published: March 04, 2017
Showing 1-10 of 10

Last Updated: 09/26/2026